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首页> 外文期刊>European review for medical and pharmacological sciences. >Low-expression of lncRNA-ANCR promotes tibial fracture healing via targeting RUNX2
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Low-expression of lncRNA-ANCR promotes tibial fracture healing via targeting RUNX2

机译:LNCRNA-ANCR的低表达促进胫骨骨折愈合通过靶向RUNX2

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OBJECTIVE: To explore the role of long non-coding ribonucleic acid-anti-differentiation non-coding ribonucleic acid (lncRNA-ANCR) in tibial fracture healing in rabbits by regulating the runt-related transcription factor 2 (RUNX2) expression. MATERIALS AND METHODS: A total of 60 healthy adult rabbits were evenly divided into Control group (n=20), Fracture group (n=20), and Lnc group (n=20). Then, RUNX2 transfection, Real Time Polymerase Chain Reaction (PCR) assay and relevant instruments were carried out and used to determine the differences in dry weight, bone mineral density, bone mechanical strength, and RUNX2 expression in tibiae among three groups of rabbits. RESULTS: Comparison of the bone mineral density in rabbit tibiae among the three groups showed that the bone mineral density was significantly lower in Fracture group than that in Control group (p0.05), and it was slightly higher in Lnc group than in Fracture group (p0.05). The dry weight of the full-length tibiae in Fracture group was significantly decreased compared with that in Control group (p0.05), and Lnc group had an increased dry weight of tibiae in comparison with Fracture group (p0.05). The maximum load, flexural strength, elastic stress, elastic strain, elastic modulus, maximum stress, and maximum strain in Fracture group were lower than those in both Control group and Lnc group (p0.05). Compared with those in Fracture group, the amount of new collagen was overtly increased in Lnc group, and that of mature collagen was decreased (p0.05). The relative expression level of RUNX2 in tibial bone tissues was evidently lower in Fracture group than that in Control group (p0.05), and it was markedly higher in Lnc group than that in Fracture group (p0.05). CONCLUSIONS: Down-regulating lncRNA-ANCR activates and triggers the expression of RUNX2 that facilitates the growth and metabolism of bone tissues to play an important role in the repair of bone tissues and promote the healing of the tibial fracture.
机译:目的:通过调节runt相关的转录因子2(RUNX2)表达,探讨长期非编码核糖核酸 - 抗分分化非编码核糖核酸(LNCRNA-ANCR)在兔中胫骨骨折愈合中的作用。材料和方法:总共60个健康的成人兔均匀分为对照组(n = 20),裂缝组(n = 20)和LNC组(n = 20)。然后,进行RUNX2转染,实时聚合酶链反应(PCR)测定和相关仪器,用于确定三组兔子中胫骨中的干重,骨密度,骨机械强度和RONX2表达的差异。结果:三组兔胫骨中骨密度的比较表明,骨折组骨密度明显低于对照组(P <0.05),LNC组略高于骨折组(P <0.05)。与对照组(P <0.05)相比,骨折组全长胫骨的干重显着降低(P <0.05),与骨折组(P <0.05)相比,LNC组对胫骨的干重增加(P <0.05)。最大载荷,弯曲强度,弹性应力,弹性应变,弹性模量,最大应力和最大菌株在裂缝组中低于对照组和LNC组(P <0.05)。与骨折组中的那些相比,LNC组在新胶原蛋白的量显着增加,成熟胶原蛋白的含量降低(P <0.05)。胫骨骨组织中Runx2的相对表达水平明显低于对照组的裂缝组(P <0.05),在LNC组中显着高于骨折组(P <0.05)。结论:降低调节LNCRNA-ancr激活并触发RUNX2的表达,促进骨组织的生长和代谢在骨组织修复中发挥重要作用,促进胫骨骨折的愈合。

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